睡眠低氧血症可预测睡眠呼吸暂停患者的死亡率:睡眠心脏健康研究的二次分析

Mohammad Masoudian Khouzani DDS, MPH , Jack Botros DDS , Mariela Padilla DDS, MEd , Richard J. Castriotta MD, FCCP
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引用次数: 0

摘要

睡眠心脏健康研究(SHHS)是一项前瞻性队列研究,旨在探讨OSA患者发生心血管疾病的危险因素,通过无人陪伴的家庭睡眠呼吸暂停测试进行诊断。我们使用这些数据来比较呼吸暂停低通气指数(AHI)和睡眠低氧血症的数量与全因死亡风险的关系。低氧血症、AHI和OSA患者死亡率之间的关系是什么?研究设计与方法我们比较了(1)AHI,(2)睡眠时间百分比与血氧饱和度的关系;85% (PERC85)和(3)睡眠时间(以分钟为单位)与氧饱和度<;85% (MIN85)伴有SHHS全因死亡风险。采用多变量logistic回归分析,并对年龄、性别、BMI、吸烟包年、基线心血管评分和治疗状态进行调整。结果sperc85与死亡风险增加相关(OR, 1.03;95% ci, 1.01-1.05;P = .003)。患者的PERC85为1%至5%,5%至20%,和>;20%的患者与PERC85的患者相比,风险逐渐增加。1% (1%-5%: or, 1.37 [95% ci, 1.02-1.83];5%-20%: or, 1.76 [95% ci, 1.07-2.86];比;20%: or, 2.93 [95% ci, 1.20-6.98];P & lt;0.05)。MIN85预测全因死亡率(OR, 1.01 [95% CI, 1.00-1.01];P = .009)。2 - 30分钟及>;30分钟的per85比30分钟的per85死亡的可能性更高。2分钟(2-30分钟):OR, 1.29 [95% CI, 1.01-1.63];比;30分钟:OR, 2.15 [95% CI, 1.22-3.76];P & lt;0.05)。AHI与死亡风险增加无关。我们的研究结果表明,睡眠低氧血症伴MIN85比AHI更能预测OSA患者的死亡率。监测氧饱和度水平和持续时间对于OSA的风险分层和治疗充分性评估可能是重要的,尽管这可能与与OSA无关的低氧血症相混淆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep Hypoxemia as a Predictor of Mortality in Patients with Sleep Apnea

Background

The Sleep Heart Health Study (SHHS) was a prospective cohort study formulated to explore the risk factors for development of cardiovascular disease in OSA, diagnosed via unaccompanied home sleep apnea test. We used these data to compare the association of the apnea-hypopnea index (AHI) and amount of sleep hypoxemia with the risk of all-cause mortality.

Research Question

What is the relationship among hypoxemia, AHI, and mortality in OSA?

Study Design and Methods

We compared the association of (1) the AHI, (2) the percentage of sleep time with oxygen saturation < 85% (PERC85), and (3) the duration of sleep (in minutes) with oxygen saturation < 85% (MIN85) with the risk of all-cause mortality in the SHHS. Multivariable logistic regression analyses were used and adjusted for age, sex, BMI, pack-years of smoking, cardiovascular score at baseline, and treatment status.

Results

PERC85 was associated with an increased risk of death (OR, 1.03; 95% CI, 1.01-1.05; P = .003). Patients with PERC85 of 1% to 5%, 5% to 20%, and > 20% showed progressively higher risks compared with those with PERC85 of < 1% (1%-5%: OR, 1.37 [95% CI, 1.02-1.83]; 5%-20%: OR, 1.76 [95% CI, 1.07-2.86]; > 20%: OR, 2.93 [95% CI, 1.20-6.98]; P < .05 for all). The MIN85 predicted all-cause mortality (OR, 1.01 [95% CI, 1.00-1.01]; P = .009). Participants with 2 to 30 min and > 30 min of PERC85 showed higher likelihoods of death vs those with PERC85 of < 2 min (2-30 mins: OR, 1.29 [95% CI, 1.01-1.63]; > 30 min: OR, 2.15 [95% CI, 1.22-3.76]; P < .05 for all). AHI was not associated with an increased risk of mortality.

Interpretation

Our findings indicate that sleep hypoxemia with MIN85 is a better predictor of mortality in OSA than AHI. Monitoring oxygen saturation levels and duration may be important for risk stratification and assessment of treatment adequacy in OSA, although this may be confounded by hypoxemia not related to OSA.
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